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- Title
Remarkable progress in cystic fibrosis—But why?
- Authors
Rang, Catherine; Wilson, John
- Abstract
The article discusses Cystic fibrosis (CF), an autosomal recessive monogenetic condition effecting 1 in 3000 live births in individuals of northern European descent and there are about 70 000 individuals with CF worldwide. Topics include access to modulator therapy from birth, effects of mutations in the gene coding for the CF transmembrane conductance regulator (CFTR), and developments in the treatment for the condition.
- Subjects
CYSTIC fibrosis; CYSTIC fibrosis transmembrane conductance regulator; BIOLOGICAL tags; EXOCRINE pancreatic insufficiency; CHLORIDE channels
- Publication
Respirology, 2019, Vol 24, Issue 1, p17
- ISSN
1323-7799
- Publication type
Article
- DOI
10.1111/resp.13440